ATG4B

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, ATG4B Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated ATG4B data layer compared with 23 for mass-spec protein and 3 for mass-spec protein.

The strongest signal is observed in lung squamous cell carcinoma (LUSC), where higher ATG4B Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated ATG4B expression acts as an unfavorable survival marker.

LUSC, COAD, and PRAD are the cancer types where ATG4B Mutation most reproducibly stratifies survival.

Mutation survival associations by lineage

Ranked by sampling consensus. AUC1 and AUC2 indicate survival in the high- and low-expression groups, respectively; the lower AUC marks the poorer-surviving group. p-values are from the log-rank test.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
LUSCOSMedianAll0.1330.762<.00112view →
COADOSMedianIII,IV0.0540.793<.0016view →
PRADDFSMedianAll0.0470.935<.0016view →
UCECOSMedianIV0.2310.592.0366view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

ATG4B–LUSC (OS)

Kaplan–Meier survival curve for ATG4B mutant vs wild-type samples in LUSC.

Open the LUSC breakdown →

Exploration